NM_001291303.3(FAT4):c.11820A>G (p.Ser3940=)
|
rs17009721
|
0.02714
|
NM_001291303.3(FAT4):c.12852C>T (p.Ser4284=)
|
rs17009819
|
0.02466
|
NM_001291303.3(FAT4):c.11488A>G (p.Lys3830Glu)
|
rs17009684
|
0.02342
|
NM_001291303.3(FAT4):c.14183G>A (p.Arg4728Lys)
|
rs72675395
|
0.01656
|
NM_001291303.3(FAT4):c.1101A>G (p.Val367=)
|
rs57692448
|
0.01498
|
NM_001291303.3(FAT4):c.14135C>G (p.Ser4712Cys)
|
rs147662558
|
0.01304
|
NM_001291303.3(FAT4):c.9876G>A (p.Gly3292=)
|
rs115219562
|
0.01168
|
NM_001291303.3(FAT4):c.8842A>G (p.Ile2948Val)
|
rs76048257
|
0.01112
|
NM_001291303.3(FAT4):c.13605G>A (p.Lys4535=)
|
rs75469760
|
0.01048
|
NM_001291303.3(FAT4):c.8544C>T (p.Ser2848=)
|
rs139132509
|
0.00802
|
NM_001291303.3(FAT4):c.11429A>G (p.His3810Arg)
|
rs114637892
|
0.00732
|
NM_001291303.3(FAT4):c.12071G>A (p.Arg4024Gln)
|
rs28515675
|
0.00726
|
NM_001291303.3(FAT4):c.4154T>C (p.Leu1385Ser)
|
rs139883132
|
0.00597
|
NM_001291303.3(FAT4):c.10853C>T (p.Thr3618Met)
|
rs111423173
|
0.00407
|
NM_001291303.3(FAT4):c.12855T>C (p.Asp4285=)
|
rs78040862
|
0.00365
|
NM_001291303.3(FAT4):c.12070C>T (p.Arg4024Trp)
|
rs138019311
|
0.00333
|
NM_001291303.3(FAT4):c.4303A>G (p.Ile1435Val)
|
rs142747281
|
0.00288
|
NM_001291303.3(FAT4):c.10390A>G (p.Ile3464Val)
|
rs147872710
|
0.00237
|
NM_001291303.3(FAT4):c.1128G>A (p.Val376=)
|
rs202216461
|
0.00236
|
NM_001291303.3(FAT4):c.524G>T (p.Arg175Leu)
|
rs143534324
|
0.00217
|
NM_001291303.3(FAT4):c.5921-14C>T
|
rs190218898
|
0.00151
|
NM_001291303.3(FAT4):c.5275A>G (p.Ile1759Val)
|
rs145639192
|
0.00145
|
NM_001291303.3(FAT4):c.8021A>T (p.Asp2674Val)
|
rs138655269
|
0.00121
|
NM_001291303.3(FAT4):c.11619C>T (p.Cys3873=)
|
rs141328606
|
0.00092
|
NM_001291303.3(FAT4):c.3682C>G (p.Gln1228Glu)
|
rs200227715
|
0.00087
|
NM_001291303.3(FAT4):c.5792A>G (p.Tyr1931Cys)
|
rs139716832
|
0.00061
|
NM_001291303.3(FAT4):c.12769G>A (p.Glu4257Lys)
|
rs143513466
|
0.00056
|
NM_001291303.3(FAT4):c.11380C>T (p.Arg3794Trp)
|
rs201859188
|
0.00020
|
NM_001291303.3(FAT4):c.1099G>A (p.Val367Ile)
|
rs747531733
|
0.00013
|
NM_001291303.3(FAT4):c.10750C>G (p.Leu3584Val)
|
rs751277769
|
0.00006
|
NM_001291303.3(FAT4):c.11906-17A>C
|
rs748245015
|
0.00006
|
NM_001291303.3(FAT4):c.9800A>G (p.His3267Arg)
|
rs773545119
|
0.00002
|
NM_001291303.3(FAT4):c.10247G>C (p.Ser3416Thr)
|
|
|
NM_001291303.3(FAT4):c.4195C>A (p.Pro1399Thr)
|
rs1486226093
|
|
NM_001291303.3(FAT4):c.739C>A (p.Pro247Thr)
|
rs191329848
|
|